CHAPS

CHAPS Basic information
Product Name:CHAPS
Synonyms:CHAPS;CHAPS (3-((3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO)PROPANESULFONATE);3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANE SULPHONATE (ULTRAPURE);3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]PROPANESULFONAT(CHAPS);3-[(3-Cholamidopropyl)dimethylammonio]-1-propanesulphonate (Ultrapure) >99.0%;CHAPS, 98+%;CHAPS extrapure;1-Propanaminium, N,N-dimethyl-N-(3-sulfopropyl)-3-[[(3a,5b,7a,12a)-3,7,12-trihydroxy-24-oxocholan-24-yl]amino]-, inner salt
CAS:75621-03-3
MF:C32H58N2O7S
MW:614.88
EINECS:616-246-2
Product Categories:Miscellaneous Biochemicals;Surfactants;Amphoteric Surfactants;Amphoteric Surfactants (for Biochemistry);Betaine Type (Surfactants);Detergents;Bile Acids;Surfactants (for Biochemistry);Ammonium Polyhalides, etc. (Quaternary);Biochemistry;Functional Materials;Quaternary Ammonium Compounds;Steroids;Buffer;detergent;Glycon Biochem
Mol File:75621-03-3.mol
CHAPS Structure
CHAPS Chemical Properties
Melting point 156-158°C (dec.)
density 1.01 g/mL at 20 °C
refractive index 1.6900 (estimate)
storage temp. -20°C
solubility H2O: 50 mg/mL at 20 °C, clear, colorless
form Crystalline Powder
color White
OdorOdorless
PH Range6
Water Solubility Soluble in water (10 mg/ml). Soluble in DMF and hot methanol.
Sensitive Hygroscopic
Merck 2044
Stability:Moisture Sensitive: Hydroscopic
InChIKeyUMCMPZBLKLEWAF-RFCNGIAKSA-N
Safety Information
Hazard Codes Xi,T
Risk Statements 36/37/38-61
Safety Statements 26-36-45-53
WGK Germany 3
3-10
HS Code 29239000
MSDS Information
CHAPS Usage And Synthesis
Chemical PropertiesCHAPS is a white crystalline powder that it is structurally similar to certain bile acids, such as taurodeoxycholic acid and taurochenodeoxycholic acid. It is sparingly soluble or insoluble in aqueous solution due to their native hydrophobicity. Chaps may be synthesized from cholic acid and is zwitterionic due to its quaternary ammonium and sulfonate groups.
UsesCHAPS is a zwitterionic nondenaturing detergent for solubilizing membrane proteins. It is used in the laboratory to dissolve biological macromolecules such as proteins. It acts as a non-denaturing solvent used in purification of membrane proteins. It is also useful in conjunction with nonionic detergents like Triton X-100. Further, it is used as a non-denaturing zwitterionic detergent for membrane biochemistry.
ApplicationCHAPS is often used as a detergent in the solubilization and purification of membrane proteins for several advantageous reasons. CHAPS detergent is non-denaturing to membrane proteins, can solubilize proteins, disaggregate protein-protein interactions. CHAPS is also useful in ion exchange chromatography and isoelectric focusing as it is zwitterionic and does not exhibit a net charge between pH 2 to 12. It is suitable for isolation of membrane proteins with the following features such as sufficient protein solubilization capability, no denaturing or inactivation of proteins, no interference with protein activities, no precipitation at 4°C, appropriate critical micelle concentrations (CMC) and micelle size, no absorption in the UV region, no toxicity and availability of detergent detection methods.
DefinitionChEBI: 3-[(3-cholamidopropyl)dimethylammonio]propane-1-sulfonate is a 1,1-diunsubstituted alkanesulfonate. It is functionally related to a cholic acid.
General DescriptionCHAPS is a stabilizing agent that can be used to prevent aggregation, precipitation or proteolysis of proteins in solution.
Biological ActivityCHAPS is a zwitterionic nondenaturing detergent for solubilizing membrane proteins. Combines the properties of both the sulfobetaine-type and bile-acid detergents.
storageRoom temperature
Purification MethodsTriturate this zwitterionic detergent (~50g) with MeOH (200ml), then triturate it with Me2CO (500mL), collect it by vacuum filtration and dry it thoroughly at ~20o. Recrystallise it at 0o from absolute MeOH followed by drying in vacuo to constant weight. It should give one spot with RF 0.32 by TLC on silica gel G in 95% MeOH/5% NH4OH and visualized with iodine vapour; the tertiary amine precursor has RF 0.40. It has low UV absorption (1% in H2O: A280nm is 0.029 and A260nm is 0.035), and the CMC (critical micellar concentration) is 8mM. It is soluble in H2O, MeOH, Me2SO but insoluble in Me2CO, MeCN, hexane, toluene and xylene. [Hjelmeland et al. Anal Biochem 130 72 1983, Matuo et al. Methods Enzymol 198 155 1991.] CHAPSO (3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate betaine) [82473-24-3] M 630.89, m 184-196o, [ ] D +19o (c 2, H2O), pKEst (1) ~<2 (acidic), pKEst(2) ~9 (basic). Dissolve this zwitterionic detergent (~ 60g) in 40% aqueous MeOH and stir it with the mixed-bed ion-exchange resin RG-501 x 8 (100g, Bio-Rad) until the pH of the supernatant is ~ 7. Filter off the resin and evaporate the filtrate to dryness under reduced pressure. Check for homogeneity by TLC on silica gel G in 95% MeOH/5% NH4OH and visualize the spot with iodine vapour (see CHAPS above). [Hjelmeland et al. Anal Biochem 130 72 1983, Matuo et al. Methods Enzymol 198 155 1991.]
CHAPS Preparation Products And Raw materials
Cyclopentanemethanol Nickel bis(sulphamidate) Sulfanilic acid N,N,N',N'-Tetramethylazodicarboxamide N-METHYL-N-OCTADECYLAMINE N-propylisononylamine CHAPS 4-Amino-benzenesulfonic acid monosodium salt 10-NONADECANOL 2,5-DIMETHYLCYCLOHEXANOL 4-Dimethylaminobenzaldehyde Heptanamide Sodium allylsulfonate Sulfamic acid N-OCTANAMIDE 3-[(3-CHOLAMIDOPROPYL)DIMETHYLAMMONIO]-1-PROPANESULFONATE HYDRATE 3-(Cholamidopropyl)-1,1-dimethamine Cocoyl amide propyldimethyl glycine

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